Variant report

Variant	rs6704231
Chromosome Location	chr1:84305432-84305433
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84281400-84316600	Weak transcription	Pancreas	Pancrea
2	chr1:84295400-84309000	Weak transcription	Primary T cells from cord blood	blood
3	chr1:84295400-84310200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:84297600-84313000	Weak transcription	Aorta	Aorta
5	chr1:84301800-84310200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr1:84305000-84306000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:84305000-84306000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr1:84305000-84306000	Enhancers	Liver	Liver
9	chr1:84305200-84305800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr1:84305200-84305800	Enhancers	NHEK	skin
11	chr1:84305200-84306000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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